Angiogenesis is a link between atherosclerosis and tumorigenesis: Role of LOX-1
Cardiovascular Drugs and Therapy, ISSN: 0920-3206, Vol: 25, Issue: 5, Page: 461-468
2011
- 25Citations
- 45Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations25
- Citation Indexes25
- 25
- CrossRef24
- Captures45
- Readers45
- 45
Article Description
Angiogenesis is defined as the formation of new blood vessels sprouting from pre-existing vessels. It plays an important role not only in physiological situations such as embryonic vascular development and wound healing, but also in pathological conditions including atherogenesis and evolution and spread of certain tumors. Lectin-like oxidized low-density lipoprotein receptor-1 (LOX-1), a receptor for oxidized low density lipoprotein (ox-LDL), is mainly expressed in endothelial cells. It has diverse physiological functions and it could be a link between atherogenesis and tumorigenesis. The risk factors for atherosclerosis like hypertension, diabetes mellitus and hyperlipidemia are associated with LOX-1. Dyslipidemia and obesity are also being recognized as risk factor for certain tumors. LOX-1 is also found to be important for maintaining the transformed state in developmentally diverse cancer cell lines and for tumor growth. There is emerging evidence that LOX-1 plays an important role in the angiogenesis process. In this review, we outline the roles of angiogenesis in atherogenesis and tumorigenesis, and describe the role of LOX-1 as a potential molecular target for blocking angiogenesis. © 2011 Springer Science+Business Media, LLC.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=83055172735&origin=inward; http://dx.doi.org/10.1007/s10557-011-6343-3; http://www.ncbi.nlm.nih.gov/pubmed/21968594; http://link.springer.com/10.1007/s10557-011-6343-3; http://www.springerlink.com/index/10.1007/s10557-011-6343-3; http://www.springerlink.com/index/pdf/10.1007/s10557-011-6343-3; https://dx.doi.org/10.1007/s10557-011-6343-3; https://link.springer.com/article/10.1007/s10557-011-6343-3
Springer Science and Business Media LLC
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